Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1513069767
Device Listing 1513069767
Listing Summary
#
Listing key
1513069767
Premarket submission
K023079
Device
NEW OUTLINE
Applicant
Anaxdent GmbH
Product code
EBG
Decision date
2002-10-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
138552
3009432160
3009432160
anax USA
1
Y
2026-01-01
406 I ST NW ARDMORE Ardmore OK US 73401